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dc.contributor.authorIngle, Arun B.en_US
dc.contributor.authorChao, Chin-Shengen_US
dc.contributor.authorHung, Wei-Chengen_US
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.date.accessioned2014-12-08T15:36:43Z-
dc.date.available2014-12-08T15:36:43Z-
dc.date.issued2014-08-01en_US
dc.identifier.issn2193-5807en_US
dc.identifier.urihttp://dx.doi.org/10.1002/ajoc.201402057en_US
dc.identifier.urihttp://hdl.handle.net/11536/25085-
dc.description.abstractThe synthesis of the O-antigen pentasaccharide repeating unit of the cell wall of Gram-negative bacteria Escherichia coli O86 is reported. The synthesis features the use of an N-formylmorpholine (NFM)-modulated glycosylation method for the construction of 1,2-cis alpha-glycosidic linkages and an [1+1+2] iterative one-pot alpha-glycosylation strategy to accelerate the assembly of the tetrasaccharide backbone.en_US
dc.language.isoen_USen_US
dc.subjectEscherichia coli O86en_US
dc.subjectglycosylationen_US
dc.subjectO-antigenen_US
dc.subjectoligosaccharidesen_US
dc.subjecttotal synthesisen_US
dc.titleChemical Synthesis of the O-Antigen Repeating Unit of Escherichia coli O86 by an N-Formylmorpholine-Modulated One-Pot Glycosylation Strategyen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ajoc.201402057en_US
dc.identifier.journalASIAN JOURNAL OF ORGANIC CHEMISTRYen_US
dc.citation.volume3en_US
dc.citation.issue8en_US
dc.citation.spage870en_US
dc.citation.epage876en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000340558500007-
dc.citation.woscount0-
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